Importance of genetic evaluation and testing in pediatric cardiomyopathy - Test2 - elhamkhani - TriplyDB

Importance of genetic evaluation and testing in pediatric cardiomyopathy

Importance of genetic evaluation and testing in pediatric cardiomyopathy

http://www.wikidata.org/entity/Q27024601

about

Toward Personalized Medicine: Does Genetic Diagnosis of Pediatric Cardiomyopathy Influence Patient Management?Diverse Phenotypic Expression of Cardiomyopathies in a Family with TNNI3 p.Arg145Trp Mutation.Evaluation of genetic causes of cardiomyopathy in childhood.Genetics of paediatric cardiomyopathies.Genomic analysis of an infant with intractable diarrhea and dilated cardiomyopathy.Genetic Testing in Pediatric Cardiomyopathy.Noncompaction cardiomyopathy and heterotaxy syndrome.

P2860

Q36057314-311D8920-8D46-4758-8263-850EA41910F4 Q37735388-59AAF46F-F23D-483B-B249-E09573B9E54B Q38588154-2C79C0DE-E922-4D19-8D76-521F004C57F5 Q39430716-9BC1F855-2C49-4F05-9E74-2577578FC957 Q45063174-A6361714-9338-472B-BB20-D18F87441EC3 Q47393959-423D4E00-C6E7-4B44-A733-E24215F49AA9 Q50235905-F37614EE-D7E8-45C8-88B5-351DEA342737

P2860

Importance of genetic evaluation and testing in pediatric cardiomyopathy

http://www.wikidata.org/entity/Q27024601

description

2014 nî lūn-bûn

@nan

2014 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Importance of genetic evaluation and testing in pediatric cardiomyopathy

@ast

Importance of genetic evaluation and testing in pediatric cardiomyopathy

@en

Importance of genetic evaluation and testing in pediatric cardiomyopathy

@nl

type

label

Importance of genetic evaluation and testing in pediatric cardiomyopathy

@ast

Importance of genetic evaluation and testing in pediatric cardiomyopathy

@en

Importance of genetic evaluation and testing in pediatric cardiomyopathy

@nl

prefLabel

Importance of genetic evaluation and testing in pediatric cardiomyopathy

@ast

Importance of genetic evaluation and testing in pediatric cardiomyopathy

@en

Importance of genetic evaluation and testing in pediatric cardiomyopathy

@nl

P1433

Q27024601-5BC5D051-915C-4913-B37D-E82A8905B105

P1476

Q27024601-67CD5420-2162-494B-BE6C-51B91E124122

P2093

Q27024601-2F303471-E84D-46A7-8F33-F31E2F45DFBC

P2860

Q27024601-07613B5C-EBF8-4007-9376-F8F420D328A0

Q27024601-099FF292-17B0-42B9-8CB3-00FFB000B25E

Q27024601-0BB64BD8-5D23-4C51-86A9-19A3D59297DC

Q27024601-0E000C90-BEAE-4388-83EA-B2C85A9B0F24

Q27024601-0FB15213-183A-446D-9652-522423B7EC2C

Q27024601-14E3B91F-A82E-4BF4-A54B-36DFE8E556CA

Q27024601-14F54CDE-42C7-4D99-9AC4-FA1964A668B4

Q27024601-1D5F53D7-F149-4852-98A7-A7931E86EDC7

Q27024601-1D6FF60D-B9BA-4401-AC57-DA646C31ED5A

Q27024601-1FEC47AC-98F4-4397-A0A8-A8DE29145853

P304

Q27024601-DA652554-7D7A-49C0-8B3E-3DDF3B30B374

P31

Q27024601-1ED43C19-F4A1-4B27-B245-A2F0B0AF2B50

P356

Q27024601-47C5F5AD-01FE-45E7-9804-608E14F2250A

P407

Q27024601-7673CB1B-1E30-4D95-B0E5-5D03EC0DC796

P433

Q27024601-63FDD8F2-A476-42D3-8466-3006704C6F45

P478

Q27024601-E615AA26-58DE-444D-814D-D130736A7D77

P577

Q27024601-7FF4E539-4229-4FEB-ADC5-A1C181FB8A77

P5875

Q27024601-222D9F73-CA67-4D93-B95D-749F54AD5C8C

P698

Q27024601-E367DDF7-5165-472D-8E2E-0DA50E2AE900

P921

Q27024601-1B46F8E9-393F-4BDA-BD9D-D803F474CE90

Q27024601-5FE2359D-E328-4DB1-95D3-08DB2CA495F5

P932

Q27024601-69F1D9D5-1527-46C3-9554-5628B48624E5

P356

WJC.V6.I11.1156

P1433

World journal of cardiology

P1476

Importance of genetic evaluation and testing in pediatric cardiomyopathy

@en

P2093

Muhammad Tariq

http://www.w3.org/2001/XMLSchema#string

P2860

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathy

Exome sequencing identifies the cause of a mendelian disorder

SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing

Targeted capture and massively parallel sequencing of 12 human exomes

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene

Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

P304

1156-65

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.4330/WJC.V6.I11.1156

http://www.w3.org/2001/XMLSchema#string

P407

P433

11

http://www.w3.org/2001/XMLSchema#string

P478

6

http://www.w3.org/2001/XMLSchema#string

P577

2014-11-26T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

268877914

http://www.w3.org/2001/XMLSchema#string

P698

25429328

http://www.w3.org/2001/XMLSchema#string

P921

Exome sequencing

P932

4244613

http://www.w3.org/2001/XMLSchema#string